The Recall Desk

State

Kentucky product recalls

19,702 recalls have nationwide distribution and so reach Kentucky. 0 additional recalls listed Kentucky specifically in their distribution scope.

About recalls in Kentucky

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kentucky consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

451–475 of 19702

  • SevereCPSC·26531·2026-06-04

    Residential Elevator Interlock Switches Recalled for Fall and Crushing Hazard

    SUNS International is recalling about 7,000 SS6291 Solenoid Interlock Switches used in residential elevators because they can become stuck, allowing the exterior door to remain unlocked and creating a risk of death or serious injury.

    Product
    SUNS SS6291 Solenoid Interlock Switches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26524·2026-06-04

    Wyze Solar Cam Pan Security Cameras recalled for fire and burn hazard

    Wyze Labs is recalling about 321,360 Solar Cam Pan security cameras because incorrect assembly instructions can cause the lithium-ion battery to overheat and catch fire. The firm has received 13 reports of overheating, six of fires, and six reports of minor burns.

    Product
    Wyze Solar Cam Pan Security Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26532·2026-06-04

    Vornado SRTH Small Room Tower Heaters Recalled for Fire Hazard

    Vornado is recalling about 255,000 SRTH small room tower heaters because the fan blade can detach, causing overheating and fire. Vornado has received 32 overheating reports, including eight fires and one smoke inhalation.

    Product
    SRTH Small Room Tower Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26527·2026-06-04

    Crenlux Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Crenlux pool drain covers violate federal safety standards and pose risks of entrapment and drowning. About 200 units sold on Amazon from June 2025 through March 2026 are affected.

    Product
    Crenlux Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26525·2026-06-04

    Little Grape Land Nursing Pillows Recalled Due to Suffocation Risk

    Little Grape Land Nursing Pillows are being recalled due to a risk of serious injury or death from suffocation. The pillows violate mandatory safety standards for nursing pillows and infant support cushions. No injuries have been reported.

    Product
    Little Grape Land Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26529·2026-06-04

    Pool Drain Covers Recalled for Entrapment and Drowning Hazards

    Broqixin pool drain covers violate federal safety standards and pose a risk of serious injury or death from entrapment and drowning. About 370 units sold on Amazon from January to April 2026 should be removed immediately.

    Product
    Broqixin Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V263000·2026-06-04

    [pending] 2025 EAST TO WEST BRAVADO

    Pending LLM rewrite. Source: NHTSA 25V263000.

    Product
    EAST TO WEST — 2025 EAST TO WEST BRAVADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V218000·2026-06-04

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    GENESIS — 2024 GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26530·2026-06-04

    Boon NURSH 8 oz Reusable Baby Bottles Recalled for Choking Hazard

    TOMY International is recalling Boon NURSH 8 oz Reusable Baby Bottles because the hard plastic outer shell can bubble or peel, creating loose plastic pieces that pose a choking hazard to young children. No injuries have been reported.

    Product
    Boon NURSH 8 oz Reusable Baby Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V264000·2026-06-04

    [pending] 2025 COACHMEN CATALINA

    Pending LLM rewrite. Source: NHTSA 25V264000.

    Product
    COACHMEN — 2025 COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26526·2026-06-04

    Children's Tiny Land Play Tents Recalled for Skin and Eye Irritation Risk

    Tiny Land Inc. is recalling about 7,500 children's play tents because fiberglass poles can shed fibers, causing skin and eye irritation. Consumers should stop using the tents immediately and contact Tiny Land for a free repair kit with plastic replacement poles.

    Product
    Children's Tiny Land Play Tents
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26528·2026-06-04

    Gudook Adult Bike Helmets Recalled for Serious Head Injury Risk

    Gudook Adult Bike Helmets (model KY-055, batch 202503, March 2025 manufacture) violate mandatory safety standards and fail to protect users in a crash, posing a serious risk of head injury or death. About 520 units sold on Amazon from May 2025 through February 2026.

    Product
    Gudook Adult Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V188000·2026-06-04

    [pending] 2025 NISSAN KICKS

    Pending LLM rewrite. Source: NHTSA 25V188000.

    Product
    NISSAN — 2025 NISSAN KICKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0551-2026·2026-06-03

    [pending] PRED MILD (PREDNISOLONE ACETATE)

    Pending LLM rewrite. Source: FDA_DRUG D-0551-2026.

    Product
    PRED MILD — PRED MILD (PREDNISOLONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0550-2026·2026-06-03

    [pending] NICOTINE (NICOTINE)

    Pending LLM rewrite. Source: FDA_DRUG D-0550-2026.

    Product
    NICOTINE — NICOTINE (NICOTINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2237-2026·2026-06-03

    [pending] Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL

    Pending LLM rewrite. Source: FDA_DEVICE Z-2237-2026.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2233-2026·2026-06-03

    [pending] Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINA

    Pending LLM rewrite. Source: FDA_DEVICE Z-2233-2026.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2238-2026·2026-06-03

    [pending] Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Cod

    Pending LLM rewrite. Source: FDA_DEVICE Z-2238-2026.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK
    Category
    Medical Device
    Distribution
    Distributed nationwide